No abstract

Elemental composition, dimensionality and morphology are the main factors that influence the catalytic activity and stability of platinum-based and noble metal alloy nanocatalysts.

The urgent need of catalysts with improved performances toward the hydrogen evolution reaction (HER) is still one of the crucial issues for the water splitting electrocatalysis. Herein, we exhibit that the HER activity of the Pd nanocubes could be improved by selecting the appropriately shaped titania nanocrystals as support. In particular, we used Pd nanoparticles with (100)-facet exposed to show that the HER performance of Pd cubes can be improved in both acidic and alkaline electrolyte media when combined on the anatase TiO2 nanocrystals. Furthermore, we have also investigated the facet effect of TiO2 on the performance in detail, which indicated stronger catalytic activity when (001)-TiO2 was used rather than (mix 101/001)-TiO2 and (101)-TiO2. The electron-transfer-induced improvement of HER activity of Pd/TiO2 was assessed by electron energy loss spectroscopy (EELS). Thereafter, the combined support materials with suitable facet exposed can give an additional adjusting path to regulate the HER activities of Pd nanocatalysts, which henceforth can further contribute to a novel way for tuning other catalysts with good electrocatalytic properties.

Hybrid faceted‐Ag3PO4/cube‐Cu2O composite materials have been fabricated and employed as oxygen reduction electrocatalysts for proton exchange membrane fuel cells (PEMFCs). The charge separation effect via the formation of PN junction has been demonstrated to boost the electrocatalysis toward oxygen reduction reaction. The as‐prepared rhombic dodecahedron‐Ag3PO4/cube‐Cu2O/C hybrid catalyst shows a mass‐specific activity of 109.80 mA/mgAg, which is about 6.4 times that of pure rhombic dodecahedron‐Ag3PO4/C catalyst (17.20 mA/mgAg). The density functional theory (DFT) calculation based on the density of states (DOS) further proved the optimal tunable effect, which is in pace with demonstration of electron transfer direction revealed by X‐ray photoelectron spectroscopy (XPS) analysis. Our work establishes a theoretical and practical basis for the rational design of newly non‐Pt hybrid catalysts, moreover, advances the future efficient application of PEMFCs.